Clinical Trial Site Management
Running a trial site means meeting protocol and regulatory requirements while caring for participants who are also patients. This course covers site operations, documentation and inspection readiness.
Course outline
What this programme covers, module by module.
- 01Trial site operations and the parties involved
- 02Site set up, feasibility and initiation
- 03Screening, informed consent and enrolment
- 04Protocol compliance, deviations and reporting
- 05Investigational product handling and accountability
- 06Source documents, the site file and data integrity
- 07Monitoring visits, audits and inspection readiness
What you will gain
- Set up a site to run a clinical trial
- Screen, consent and enrol participants properly
- Follow protocol and document deviations
- Manage investigational product and its accountability
- Maintain the site file to inspection standard
- Prepare for monitoring visits and audits
Who should attend
- Clinical research coordinators
- Principal and site investigators
- Research nurses and study staff
- Quality staff supporting research
Upcoming sessions
| Date | City | Duration | Fees | Book |
|---|---|---|---|---|
| 9 to 13 Nov 2026 | London | 5 Days | US$1,800 | |
| 30 Nov to 4 Dec 2026 | Dubai | 5 Days | US$1,800 | |
| 11 to 15 Jan 2027 | Pretoria | 5 Days | R18,000 | |
| 25 to 29 Jan 2027 | Durban | 5 Days | R18,000 | |
| 5 to 9 Apr 2027 | Cape Town | 5 Days | R18,000 | |
| 14 to 18 Jun 2027 | Johannesburg | 5 Days | R18,000 |
Fees are per delegate and exclude VAT. Public intakes are confirmed once minimum numbers are met. We also deliver this course on your own schedule, in-house or live online.
Enquire about this course
Register your team or ask for a tailored in-house quote. We reply within one working day.
WhatsApp usCourse brochure (PDF)- Fees from
- R18,000 per delegate
- Duration
- 5 Days
- Field
- Healthcare & Hospital Management
- Formats
- In-house, public, online
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